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PATL2 中的新突变导致卵母细胞生发泡阻滞引起的女性不孕。

Novel mutations in PATL2 cause female infertility with oocyte germinal vesicle arrest.

机构信息

Center for Reproductive Medicine, Department of Obstetrics and Gynecology, Anhui Provincial Hospital Affiliated to Anhui Medical University, Hefei 230001, Anhui, China.

School of Life Science, Anhui Medical University, Hefei 230022, China.

出版信息

Hum Reprod. 2018 Jun 1;33(6):1183-1190. doi: 10.1093/humrep/dey100.

Abstract

STUDY QUESTION

Do PATL2 mutations account for female infertility with oocyte germinal vesicle (GV) arrest?

SUMMARY ANSWER

Four of nine independent families with oocyte GV arrest were identified with biallelic PATL2 mutations, suggesting that these mutations may be responsible for oocyte maturation arrest in primary infertile women.

WHAT IS KNOWN ALREADY

Recently, two independent studies have demonstrated that infertility in some women with oocyte maturation arrest at the GV stage was caused by biallelic mutations in PATL2. PATL2 encodes protein PAT1 homolog 2, an RNA-binding protein that may act as a translational repressor.

STUDY DESIGN, SIZE, DURATION: In this study, nine unrelated primary infertile females presenting with oocyte GV arrest were recruited during the treatment of early rescue ICSI or ICSI from January 2013 to December 2016.

PARTICIPANTS/MATERIALS, SETTING, METHODS: Genomic DNA was isolated from blood samples obtained from all nine affected individuals and all of their available family members. All the coding regions of PATL2 were sequenced by Sanger sequencing. The pathogenicity of the identified variants and their possible effects on the protein were evaluated in silico.

MAIN RESULTS AND THE ROLE OF CHANCE

Five novel point mutations and one recurrent splicing mutation in PATL2 were identified in four of nine (44.4%) unrelated patients. We found a consanguineous family with a homozygous missense mutation in two affected sisters, and their fertile brother. There were no clear phenotypic differences in oocytes between the patient with the homozygous missense mutation, patients with nonsense mutations and undiagnosed patients.

LARGE SCALE DATA

n/a.

LIMITATIONS, REASONS FOR CAUTION: The function of PATL2 remains largely unknown. Both the exact pathogenic mechanism(s) of mutated PATL2 causing human oocyte maturation arrest and the strategies to overcome this condition should be further investigated in the future.

WIDER IMPLICATIONS OF THE FINDINGS

According to our data, mutations in PATL2 account for 44.4% of the individuals with oocyte GV arrest. Our study further confirms that PATL2 is required for human oocyte maturation and female fertility, which indicates a potential prognostic value of testing for PATL2 mutations in primary infertile women with oocyte maturation arrest.

STUDY FUNDING/COMPETING INTEREST(S): Natural Science Foundation of Anhui Province (1808085MH241), National Natural Science Foundation of China (81401251 and 81370757) and Central Guided Local Development of Science and Technology Special Fund (2016080802D114) supported this study. None of the authors have any competing interests.

摘要

研究问题

PATL2 突变是否导致卵母细胞生发泡(GV)阻滞的女性不孕?

总结答案

在 9 个独立的卵母细胞 GV 阻滞家庭中,有 4 个家庭存在双等位基因 PATL2 突变,这表明这些突变可能导致原发性不孕女性的卵母细胞成熟阻滞。

已知情况

最近,两项独立的研究表明,一些卵母细胞成熟阻滞在 GV 期的女性不孕是由 PATL2 的双等位基因突变引起的。PATL2 编码 PAT1 同源物 2 蛋白,这是一种 RNA 结合蛋白,可能作为翻译抑制剂。

研究设计、大小、持续时间:在这项研究中,2013 年 1 月至 2016 年 12 月,在早期救援 ICSI 或 ICSI 治疗期间,招募了 9 名患有卵母细胞 GV 阻滞的原发性不孕女性。

参与者/材料、地点、方法:从所有 9 名受影响个体及其所有可利用的家庭成员的血液样本中分离基因组 DNA。通过 Sanger 测序对 PATL2 的所有编码区进行测序。对鉴定出的变异的致病性及其对蛋白质的可能影响进行了计算机预测分析。

主要结果和机会的作用

在 9 名无关患者中的 4 名(44.4%)中发现了 PATL2 中的 5 个新的点突变和 1 个重复剪接突变。我们发现了一个有亲缘关系的家庭,其中 2 名受影响的姐妹及其生育能力正常的兄弟为纯合错义突变。携带纯合错义突变的患者、携带无义突变的患者和未确诊患者的卵母细胞之间没有明显的表型差异。

大规模数据

无。

局限性、谨慎的原因:PATL2 的功能仍知之甚少。未来应进一步研究突变的 PATL2 导致人类卵母细胞成熟阻滞的确切致病机制(多个)和克服该状况的策略。

研究结果的广泛意义

根据我们的数据,PATL2 突变占卵母细胞 GV 阻滞个体的 44.4%。我们的研究进一步证实,PATL2 是人类卵母细胞成熟和女性生育所必需的,这表明在卵母细胞成熟阻滞的原发性不孕女性中检测 PATL2 突变具有潜在的预后价值。

研究资金/竞争利益:安徽省自然科学基金(1808085MH241)、国家自然科学基金(81401251 和 81370757)和中央引导地方科技发展专项资金(2016080802D114)支持了这项研究。作者均无任何竞争利益。

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